Utility of Gene Test Analysis for Diagnosis, Prognosis and Treatment of Patients With Genetic Arrhythmic Heart Disease: the ARRHYTHMIC GENE-HEART

The goal of this observational study is to enroll all patients evaluated at the specialized Cardiogenetic Center within the Cardiology Department of the University of Ferrara, Italy. The primary aim of the registry is to collect comprehensive clinical, genetic, and electrophysiological data from individuals with suspected or confirmed arrhythmogenic conditions. By systematically documenting patient demographics, family history, clinical presentations, diagnostic findings, and treatment outcomes, the registry seeks to enhance our understanding of the genetic basis and clinical implications of genetically driven arrhythmias and systemic syndromes. This registry will facilitate long-term follow-up of enrolled patients to assess the natural history of arrhythmogenic disorders and the effectiveness of various therapeutic interventions. Additionally, it aims to identify potential risk factors associated with adverse outcomes, such as sudden cardiac death or major arrhythmic events.

NCT Number	NCT06898307
Lead Sponsor	University Hospital of Ferrara
Conditions	Genetic Disease, Cardiac Disease, Cardiac Arrhythmias, Genetic Disorder, Cardiology
Enrollment	200 participants
Start Date	2017-11-01
Primary Completion	2025-11-01 (estimated)
Study Completion	2035-11-01 (estimated)
Updated on ClinicalTrials.gov	2025-03-27